drugset / Trial / NCT01892384

Safety and Tolerability of BI 409306 in Patients With Schizophrenia

NCT01892384

Phase 1 Completed 40 enrolled Boehringer Ingelheim
RandomizedParallel-groupDouble-blindTreatment

Summary

The primary objective of the current study is to investigate the safety and tolerability of BI 409306 in schizophrenic patients following oral administration of multiple low, medium, and high doses over 14 days. A secondary objective is the exploration of the pharmacokinetics and pharmacodynamics of BI 409306 in schizophrenic patients.

Timeline

Start
2013-06-28
Primary completion
2013-12-05
Completion
2013-12-05

Drugs

EvaluationDrugModalityDoseRoute
Subject OSORESNONTRINE Small molecule 25 mg Oral
Subject OSORESNONTRINE Small molecule 50 mg Oral
Subject OSORESNONTRINE Small molecule 100 mg Oral

Indications